EP0348091A1 - Aerosol composition - Google Patents

Aerosol composition Download PDF

Info

Publication number
EP0348091A1
EP0348091A1 EP89305990A EP89305990A EP0348091A1 EP 0348091 A1 EP0348091 A1 EP 0348091A1 EP 89305990 A EP89305990 A EP 89305990A EP 89305990 A EP89305990 A EP 89305990A EP 0348091 A1 EP0348091 A1 EP 0348091A1
Authority
EP
European Patent Office
Prior art keywords
powder
poe
spray
acid
aerosol composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP89305990A
Other languages
German (de)
French (fr)
Other versions
EP0348091B1 (en
Inventor
Osamu C/O Shiseido Laboratories Moro
Shuya C/O Shiseido Laboratories Tamaki
Toshihiko C/O Shiseido Laboratories Nakane
Tsunehiko C/O Shiseido Laboratories Iwai
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shiseido Co Ltd filed Critical Shiseido Co Ltd
Publication of EP0348091A1 publication Critical patent/EP0348091A1/en
Application granted granted Critical
Publication of EP0348091B1 publication Critical patent/EP0348091B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/30Materials not provided for elsewhere for aerosols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/046Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00Anti-perspirants or body deodorants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41Particular ingredients further characterized by their size
    • A61K2800/412Microsized, i.e. having sizes between 0.1 and 100 microns
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/60Particulates further characterized by their structure or composition
    • A61K2800/61Surface treated
    • A61K2800/62Coated
    • A61K2800/624Coated by macromolecular compounds

Definitions

  • the present invention relates to an aerosol composition having a very good dispersibility and an excellent useability due to a composite powder formulated therein.
  • the aerosol composition of the present invention can be utilized in such fields as drugs, quasi-drugs, cosmetics, sterilizers, and lubricants.
  • a powder spray comprising a powder dispersed in a liquefied gas propellant is used as a dry shampoo, food powder, sterilizer, lubricator, and dry type antisweat agent.
  • the dry type antisweat agent presently used is widely sold on the market.
  • a Freon gas is widely used as the propellant for these powder sprays, due to its ease of handling.
  • the powder spray gas generally contains, as the lubricator, talc, mica, silica, and spherical nylon, as a sweat preventive and deodorant, and powder of aluminum chloride, aluminum hydroxychloride, zinc oxide, and hydroxyapatite formulated therein.
  • an object of the present invention is to obviate the above-mentioned problems and to provide an aerosol composition having an excellent dispersibility and useability even if Freon gas is not used or the amount of the Freon gas is restricted.
  • an aerosol composition comprising at least one propellant selected from the group consisting of propane, isobutane, n-butane, and a liquefied petroleum gas (abbreviated hereinafter as "LPG") which is a mixture thereof, a chlorinated hydrocarbon and dimethyl ether, and a composite powder.
  • a propellant selected from the group consisting of propane, isobutane, n-butane, and a liquefied petroleum gas (abbreviated hereinafter as "LPG") which is a mixture thereof, a chlorinated hydrocarbon and dimethyl ether, and a composite powder.
  • LPG liquefied petroleum gas
  • an aerosol composition comprising at least are propellant selected from the group consisting of propane, n-butane, and isobutane, at least one solvent selected from the group consisting of n-pentane, isopentane, and n-hexane, and a composite powder.
  • the composite powder usable in the present invention comprises one or more coating powder which becomes a sheath (hereinafter abbreviated as sheath powder) attached as a composite around the powder which becomes the core (hereinafter abbreviated as the core powder).
  • the sheath powder can be selected from among inorganic powders and organic powders as desired.
  • any desired organic powder with an average particle size of 0.1 to 100 u.m can be used, and the powder used for the core can be in the form of a spherical, plate, granular, or needle, but in view of the feeling on the skin during use of the aerosol composition, the spheriod, granular or plate form is preferred.
  • Typical examples of the core powder of the composite powder are polyamides such as nylon 6, nylon 12, nylon 46, and nylon 66; polyolefins such as polyethylene and polypropylene; polystyrene; polyesters such as polyethylenenterephthalate and polycarbonate; acrylic resins such as polymethyl methacrylate and butyl acrylate-MMA copolymer; epoxy resins such as cured bisphenol A-epichlorohydrin copolymer; fluorine type resins such as polytetrafluoroethylene; silicone type resins such as methylpolysioxane and crosslinked dimethylpolysiloxane; phenolic resins such as benzoguanamine resin; vinyl resins such as polyvinyl chloride and polyvinyl methyl ether; polyurethane; cellulose; chitin; chitosan; fibroin; keratin; natural rubber; and so on.
  • polyamides such as nylon 6, nylon 12, nylon 46, and nylon 66
  • the sheath powder which is attached to the core powder to form the comosite powder may have an average particle size of 1/5 or less, preferably 1/10 or less, of that of the core powder. If the average particle size of the sheath powder is larger than 1/5 of the average particle size of the core powder, the elimination stability of the sheath powder will be extremely poor.
  • sheath powder usable in the present invention include, as inorganic powders in general, anhydrous silicic acid, magnesium silicate, talc, kaolin, bentonite, aerosil, mica, mica titanium, bismuth oxychloride, zirconium oxide, magnesium oxide, zinc oxide, titanium oxide, light calcium carbonate, heavy calcium carbonate, light magnesium carbonate, heavy magnesium carbonate, yellow iron oxide, red iron oxide, black iron oxide, ultramarine, carbon black, caramine hydroxyapatite, magnesium al- uminometasilicate, magnesium aluminosilicate, aluminum hydroxychloride, aluminum chloride, aluminum sulfate, aluminum citrate, aluminum acetate, basic aluminum chloride, aluminum phenolsulfonate, aluminum ,8-naphtholdisulfonate, lead acetate, sodium perborate, aluminum zirconium octachlorohydrate, aluminum zirconium pentachlorohydrate, aluminum zirconium te
  • Red color No. 202 Red color No. 204, Red color No. 205, Red color No. 220, Red color No. 226, Red color No. 228, Red color No. 405, Orange color No. 203, Orange color No. 204, Yellow color No. 205, Yellow color No. 401, and Blue color No. 404; zirconium, barium or aluminum lake such as Red color No. 3, Red color No. 104, Red color No. 106, Red color No. 227, Red color No. 230, Red color No. 401, Red color No. 505, Orange color No. 205, Yellow color No. 4, Yellow color No. 5, Yellow color No. 202, Yellow color No. 203, Green color No. 3 and Blue color No.
  • polyamides such as nylon 6, nylon 12, and nylon 66
  • polyolefins such as polyethylene and polypropylene
  • polystyrene polyesters such as polyethyleneterephthalate and polycarbonate
  • acrylic resins such as polymethyl methacrylate and butyl acrylate-MMA copolymer
  • epoxy resins such as cured bisphenol A-epichlorohydrin copolymer
  • fluorine type resins such as polytetrafluoroethylene
  • silicone type resins such as methylpolysioxane and crosslinked dimethylpolysiloxane
  • phenolic resins such as benzoguanamine resin
  • vinyl resins such as polyvinyl chloride and polyvinyl methyl ether
  • polyurethane cellulose; chitin; chitosan; fibroin; keratin; natural rubber
  • metalic soaps such as aluminum stearate, calcium stearate, magnesium stearate, zinc stearate, aluminum myristate
  • the composite powder can be prepared by mixing the core powder and the sheath powder by the dry process or the wet process.
  • the mixing device there may be employed various mixing devices or pulverization devices such as a ball mill, pot mill, automated mortar, grinder, attritor, sand mill, ongmill, hybridizer, cosmomizer, mechanofusion system, and hybridization system.
  • the mixing ratio of the core powder to the sheath powder may be, in terms of weight ratio, 0.1 to 200 parts, preferably 1 to 200 parts of the outer wall powder, per 100 parts of the core powder. At a level of less than 0.1 part, the effect of the sheath powder cannot be exhibited. When a powder surface modifier is used, it is used in an amount of 0.01 % to 10% by weight, based upon the core powder and the sheath powder.
  • the use of the composite powder having a modified surface is preferable from the viewpoint of the effects thereof.
  • the composite powder is prepared after the core powder and/or the sheath powder are surface modified; the composite powder is prepared by adding a surface modifier to the core powder and the sheath powder during the composite powder preparation step; and the surface modification is effected after the preparation of the composite powder and the like.
  • Typical examples of the surface modifier include oils such as ester oils, hydrocarbon oils, fatty acids, and silicone oils (e.g., methylhydrogen polysiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane, dimethylpolysiloxane, methylphenylpolysiloxane); waxes such as whale wax, Japan wax, shellac, beeswax, lanolin, carnauba wax, and canderilla; coupling agents such as silane coupling agents (e.g., vinyl trichrolosilane, triethoxy vinylsilane, 3-chloropropyl trimethoxysilane); sillylating agents (e.g., trimethylchloro silane, hexamethyl disilazane, diethylamino trimethyl silane), titanate coupling agents (e.g., methyltrichloro titanium, isopropyltriisostearoyl titanate, tetraoctyl bis (
  • polyamine forming monomers such as caprolactum
  • polyolefin forming monomers such as ethylene and propylene
  • styrene monomers polyester forming monomers such as divalent aromatic phenols and bis phenol A
  • acryl resin forming monomers such as methyl methacrylate, methacrylic acid, butyl methacrylate
  • epoxy resin monomers such as bisphenol A and epichlorohydrin
  • fluorine resin monomers silicone resin monomers
  • surfactants such as alkylallyl sulfonates, sulfuric acid ester salts of higher alcohols, phosphoric acid ester salts of higher alcohols
  • silicone surfactants such as polyether modified silicone, amino'modified silicone, alkyl modified silicone, alcohol modified silicone, and carboxylic acid modified silicone
  • fluorine surfactants such as perfluoroalkyl carboxylic acid salts, perfluoroalkyl phosphoric acid esters, perfluoroalkyl carboxylic acid salts, perfluor
  • any connectional modification methods may be used in the present invention. Examples of such methods are modification by coating, topochemical modification, mechanochemical modification, modification by encapsulation, radiation modification, and plasma irradiation modification. These methods are carried out under, for example, the vapor phase, the liquid phase or in vacuo. Furthermore, the composite powder may be modified only by, for example, plasma irradiation, without using the surface modifier.
  • the amount of the composite powder formulated in the present invention is preferably 0.1 % to 30% by weight in the total amount of the aerosol composition, more preferably 0.3% to 20% by weight: If the amount is less than 0.1 %, the effect required from the powder formulation cannot be obtained, and the effect will be unchanged if it is formulated in excess of 30% by weight.
  • the propellant usable in the present invention is one or more of propane, isobutane, n-butane, and LPG, which is a mixture thereof, chlorinated hydrocarbons such as methyl chloride and methylene chloride and dimethyl ether, and these propellants can be further used in combination with freon gases such as Freon 11, Freon 12, Freon 21, Freon 113, and Freon 114.
  • solvents examples include alcohol, n-pentane, isopentane, n-hexane, cyclohexane, isohexane, n-heptane, isooctane, 2,2-dimethylbutane, petroleum ether, petroleum benzene, ligroin, 2-pentene, methyl ethyl ether, and diethyl ether.
  • inner pressure is 0.1 to 2.5 kg/cm 2 G (gauge) at a temperature of 20 C.
  • the amount of propellant formulated is preferably 5 to 99% by weight of the total amount of the aerosol composition, more preferably 15 to 95% by weight. A good jetting state cannot be obtained at a level of less than 5% by weight.
  • composition of the present invention in addition to the above components, any of the optional components known in the art can be formulated.
  • formulation components include water; oils and fats such as avocado oil, almond oil, olive oil, grapeseed oil, sesame oil, Sasanqua oil, safflower oil, soybean oil, Tsubaki (camellia) oil, corn oil, rapeseed oil, persic oil, castor oil, sunflower oil, cottonseed oil, peanut oil, cacao oil, palm oil, coconut oil, tallow, fish fat, hardened oil, turtle oil, lard, mink oil, and egg yolk oil; waxes such as whale wax, shellac, beeswax, lanolin, liquid lanolin, carnauba wax, and canderilla wax; hydrocarbons such as liquid paraffin, liquid polyisobutylene, squalane, pristane, petrolatum, paraffin, and ceresin; silicone oils such as dimethyl polysiloxane, methyl phenyl polysiloxane, methylhydrogen polysiloxane, octamethyl cyclo tetrasi
  • the present invention provides an aerosol composition having an excellent powder dispersibility and useability by reducing the amount of Freon gas or without using Freon gas, and thus meets current requirements to restrict the use of this gas due to its influence on the ozone layer.
  • Powder and a propellant were filled in an aerosol glass bottle, and after shaking, the time in which the powder sedimented at the bottom of the bottle was measured.
  • Table 1 shows Examples and Comparative Examples.
  • a valve was mounted and crimped, and the components (6) to (8) were filled under pressure to obtain a deodorant spray.
  • the spray had a good powder dispersibility and useability.
  • the mixture was filled in an aerosol can and a valve was mounted and crimped. After crimping, (7) was filled under pressure to obtain a powder cologne spray. The spray was found to have a good powder dispersibility and useability.
  • the components (1) to (6) were homogeneously mixed and then filled in a aerosol can, and a valve was mounted and crimped, followed by filling (7) and (8) to obtain a deodorant powder spray.
  • the spray was found to have a good powder dispersibility and useability.
  • the mixture was filled in an aerosol can, and a valve was mounted and crimped, followed by filling (6) and (7) under pressure to obtain a powder spray.
  • the spray was found to have a good powder dispersibility and useability.
  • a solution of (2) to (4) dissolved in the components (1) and (5) was filled in an aerosol can and a valve was mounted and crimped, followed by filling (6) and (7) under pressure to obtain a powder spray for systemic use.
  • the spray was found to have a good powder dispersibility and useability.
  • the mixture was filled in an aerosol can.
  • a valve was mounted and crimped, followed by filling (5) and (6) under pressure to obtain a deodorant powder spray.
  • the spray was found to have a good powder dispersibility and useability.
  • a valve was mounted and crimped, and the component (6) was filled under pressure to obtain a deodorant spray.
  • the spray obtained was found to have a good powder dispersibility, useability, and deodorizing property.
  • the mixture was filled in an aerosol can, and a valve was mounted and crimped, followed by filling (6) and (7) under pressure to obtain a powder spray.
  • the spray was found to have a good powder dispersibility and useability.
  • the components (1) and (2) and the components (3) and (4) were separately uniformly mixed.
  • the resultant mixtures and the component (5) were then filled in an aerosol can, and a valve was mounted and crimped, followed by filling the component (6) under pressure to obtain a powder spray.
  • the components (1) to (3) and the components (4) and (5) were separately uniformly mixed and then filled, together with the component (6), in an aerosol can, and a valve was mounted and crimped, followed by filling the component (7) under pressure to obtain a foot spray.

Abstract

An aerosol composition containing a composite powder and one or more of propane, isobutane, n-butane and a liquefied petroleum gas (i.e., LPG) which is a mixture thereof, a chlorinated hydrocarbon and dimethyl ether.

Description

    BACKGROUND OF THE INVENTION 1. Field of the Invention
  • The present invention relates to an aerosol composition having a very good dispersibility and an excellent useability due to a composite powder formulated therein. The aerosol composition of the present invention can be utilized in such fields as drugs, quasi-drugs, cosmetics, sterilizers, and lubricants.
  • 2. Description of the Related Art
  • Usually, a powder spray comprising a powder dispersed in a liquefied gas propellant is used as a dry shampoo, food powder, sterilizer, lubricator, and dry type antisweat agent. The dry type antisweat agent presently used is widely sold on the market.
  • A Freon gas is widely used as the propellant for these powder sprays, due to its ease of handling.
  • Currently, because of the influence of this gas on the ozone layer, there is movement to restrict the use of Freon gas, and the present trend is toward a reduction of the amount of Freon gas used or finding a substitute therefor.
  • The powder spray gas generally contains, as the lubricator, talc, mica, silica, and spherical nylon, as a sweat preventive and deodorant, and powder of aluminum chloride, aluminum hydroxychloride, zinc oxide, and hydroxyapatite formulated therein.
  • If, however, the use of Freon (i.e., "CFC") gas as the propellant is restricted, the dispersibility of the powder is poor when these powders are formulated, and even when used after strong shaking, the powder may be sedimented during spraying, and thus it is not possible to ensure spraying for a relatively long period, of a uniform composition.
  • SUMMARY OF THE INVENTION
  • Accordingly, an object of the present invention is to obviate the above-mentioned problems and to provide an aerosol composition having an excellent dispersibility and useability even if Freon gas is not used or the amount of the Freon gas is restricted.
  • Other objects and advantages of the present invention will be apparent from the following description.
  • In accordance with the present invention, there is provided an aerosol composition comprising at least one propellant selected from the group consisting of propane, isobutane, n-butane, and a liquefied petroleum gas (abbreviated hereinafter as "LPG") which is a mixture thereof, a chlorinated hydrocarbon and dimethyl ether, and a composite powder.
  • In accordance with the present invention, there is also provided an aerosol composition comprising at least are propellant selected from the group consisting of propane, n-butane, and isobutane, at least one solvent selected from the group consisting of n-pentane, isopentane, and n-hexane, and a composite powder.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The composite powder usable in the present invention comprises one or more coating powder which becomes a sheath (hereinafter abbreviated as sheath powder) attached as a composite around the powder which becomes the core (hereinafter abbreviated as the core powder). The sheath powder can be selected from among inorganic powders and organic powders as desired.
  • As the core powder of the composite powder usable in the present invention, any desired organic powder with an average particle size of 0.1 to 100 u.m can be used, and the powder used for the core can be in the form of a spherical, plate, granular, or needle, but in view of the feeling on the skin during use of the aerosol composition, the spheriod, granular or plate form is preferred.
  • Typical examples of the core powder of the composite powder are polyamides such as nylon 6, nylon 12, nylon 46, and nylon 66; polyolefins such as polyethylene and polypropylene; polystyrene; polyesters such as polyethylenenterephthalate and polycarbonate; acrylic resins such as polymethyl methacrylate and butyl acrylate-MMA copolymer; epoxy resins such as cured bisphenol A-epichlorohydrin copolymer; fluorine type resins such as polytetrafluoroethylene; silicone type resins such as methylpolysioxane and crosslinked dimethylpolysiloxane; phenolic resins such as benzoguanamine resin; vinyl resins such as polyvinyl chloride and polyvinyl methyl ether; polyurethane; cellulose; chitin; chitosan; fibroin; keratin; natural rubber; and so on.
  • The sheath powder, which is attached to the core powder to form the comosite powder may have an average particle size of 1/5 or less, preferably 1/10 or less, of that of the core powder. If the average particle size of the sheath powder is larger than 1/5 of the average particle size of the core powder, the elimination stability of the sheath powder will be extremely poor.
  • Typical examples of the sheath powder usable in the present invention include, as inorganic powders in general, anhydrous silicic acid, magnesium silicate, talc, kaolin, bentonite, aerosil, mica, mica titanium, bismuth oxychloride, zirconium oxide, magnesium oxide, zinc oxide, titanium oxide, light calcium carbonate, heavy calcium carbonate, light magnesium carbonate, heavy magnesium carbonate, yellow iron oxide, red iron oxide, black iron oxide, ultramarine, carbon black, caramine hydroxyapatite, magnesium al- uminometasilicate, magnesium aluminosilicate, aluminum hydroxychloride, aluminum chloride, aluminum sulfate, aluminum citrate, aluminum acetate, basic aluminum chloride, aluminum phenolsulfonate, aluminum ,8-naphtholdisulfonate, lead acetate, sodium perborate, aluminum zirconium octachlorohydrate, aluminum zirconium pentachlorohydrate, aluminum zirconium tetrachlorohydrate, aluminum zirconium trichlorohydrate, and zirconium chlorohydrate; as organic pigments, pearl pigments such as mica coated with titanium oxide, bismuth oxychloride coated with titanium oxide, talc coated with titanium oxide, fish scale, mica coated with colored titanium oxide; metal powder pigments such as aluminum powder and copper powder; organic pigments such as Red color No. 201, Red color No. 202, Red color No. 204, Red color No. 205, Red color No. 220, Red color No. 226, Red color No. 228, Red color No. 405, Orange color No. 203, Orange color No. 204, Yellow color No. 205, Yellow color No. 401, and Blue color No. 404; zirconium, barium or aluminum lake such as Red color No. 3, Red color No. 104, Red color No. 106, Red color No. 227, Red color No. 230, Red color No. 401, Red color No. 505, Orange color No. 205, Yellow color No. 4, Yellow color No. 5, Yellow color No. 202, Yellow color No. 203, Green color No. 3 and Blue color No. 1; as organic powders, polyamides such as nylon 6, nylon 12, and nylon 66; polyolefins such as polyethylene and polypropylene; polystyrene; polyesters such as polyethyleneterephthalate and polycarbonate; acrylic resins such as polymethyl methacrylate and butyl acrylate-MMA copolymer; epoxy resins such as cured bisphenol A-epichlorohydrin copolymer; fluorine type resins such as polytetrafluoroethylene; silicone type resins such as methylpolysioxane and crosslinked dimethylpolysiloxane; phenolic resins such as benzoguanamine resin; vinyl resins such as polyvinyl chloride and polyvinyl methyl ether; polyurethane; cellulose; chitin; chitosan; fibroin; keratin; natural rubber; metalic soaps such as aluminum stearate, calcium stearate, magnesium stearate, zinc stearate, aluminum myristate, calcium, myristate, magnesium myristate, zinc myristate, aluminum paimitate, calcium palmitate, magnesium palmitate, zinc palmitate, zinc laurate, zinc undecylenate and calcium acetate; chlorophyll; tannin powder, and flavonoid.
  • As the method of preparing the composite powder to be used in the present invention, for example, the composite powder can be prepared by mixing the core powder and the sheath powder by the dry process or the wet process. As the mixing device, there may be employed various mixing devices or pulverization devices such as a ball mill, pot mill, automated mortar, grinder, attritor, sand mill, ongmill, hybridizer, cosmomizer, mechanofusion system, and hybridization system.
  • The mixing ratio of the core powder to the sheath powder may be, in terms of weight ratio, 0.1 to 200 parts, preferably 1 to 200 parts of the outer wall powder, per 100 parts of the core powder. At a level of less than 0.1 part, the effect of the sheath powder cannot be exhibited. When a powder surface modifier is used, it is used in an amount of 0.01 % to 10% by weight, based upon the core powder and the sheath powder.
  • In the practice of the present invention, the use of the composite powder having a modified surface is preferable from the viewpoint of the effects thereof. As a method of preparing the surface modified composite powder, the composite powder is prepared after the core powder and/or the sheath powder are surface modified; the composite powder is prepared by adding a surface modifier to the core powder and the sheath powder during the composite powder preparation step; and the surface modification is effected after the preparation of the composite powder and the like.
  • Typical examples of the surface modifier include oils such as ester oils, hydrocarbon oils, fatty acids, and silicone oils (e.g., methylhydrogen polysiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane, dimethylpolysiloxane, methylphenylpolysiloxane); waxes such as whale wax, Japan wax, shellac, beeswax, lanolin, carnauba wax, and canderilla; coupling agents such as silane coupling agents (e.g., vinyl trichrolosilane, triethoxy vinylsilane, 3-chloropropyl trimethoxysilane); sillylating agents (e.g., trimethylchloro silane, hexamethyl disilazane, diethylamino trimethyl silane), titanate coupling agents (e.g., methyltrichloro titanium, isopropyltriisostearoyl titanate, tetraoctyl bis (ditridecyl phosphite) titanate, bis(dioctyl pyrophosphate)-ethylene titanate); monomers forming synthetic polymers (e.g. polyamine forming monomers such as caprolactum), polyolefin forming monomers such as ethylene and propylene, styrene monomers, polyester forming monomers such as divalent aromatic phenols and bis phenol A, acryl resin forming monomers such as methyl methacrylate, methacrylic acid, butyl methacrylate, epoxy resin monomers such as bisphenol A and epichlorohydrin, fluorine resin monomers, silicone resin monomers; surfactants such as alkylallyl sulfonates, sulfuric acid ester salts of higher alcohols, phosphoric acid ester salts of higher alcohols; silicone surfactants such as polyether modified silicone, amino'modified silicone, alkyl modified silicone, alcohol modified silicone, and carboxylic acid modified silicone; fluorine surfactants such as perfluoroalkyl carboxylic acid salts, perfluoroalkyl phosphoric acid esters, perfluoroalkyl carboxylic acid salts, perfluoroalkyl trimethylammonium salts, perfluoroalkyl betains, perfluoroalkylamine oxides, and perfluoroalkyl ethylene oxide addition products; metal soaps such as aluminum stearate, calcium stearate, magnesium stearate, zinc stearate, aluminum myristate, calcium myristate, magnesium myristate, zinc myristate, aluminum palmitate, calcium palmitate, magnesium palmitate, zinc palmitate, zinc laurate, zinc undecylate, and calcium acetate; silicone resins; silicone rubber; gelatin; collagen; keratin; and fibroin.
  • As the surface modification method, any connectional modification methods may be used in the present invention. Examples of such methods are modification by coating, topochemical modification, mechanochemical modification, modification by encapsulation, radiation modification, and plasma irradiation modification. These methods are carried out under, for example, the vapor phase, the liquid phase or in vacuo. Furthermore, the composite powder may be modified only by, for example, plasma irradiation, without using the surface modifier.
  • The amount of the composite powder formulated in the present invention is preferably 0.1 % to 30% by weight in the total amount of the aerosol composition, more preferably 0.3% to 20% by weight: If the amount is less than 0.1 %, the effect required from the powder formulation cannot be obtained, and the effect will be unchanged if it is formulated in excess of 30% by weight.
  • The propellant usable in the present invention is one or more of propane, isobutane, n-butane, and LPG, which is a mixture thereof, chlorinated hydrocarbons such as methyl chloride and methylene chloride and dimethyl ether, and these propellants can be further used in combination with freon gases such as Freon 11, Freon 12, Freon 21, Freon 113, and Freon 114.
  • When Freon gas is used in combination, if the average specific gravity is 1.2 or less, the required dispersibility effect is obtained. Accordingly, when the specific gravity of the propellant becomes 1.2 or less, if the powder formulated in the powder spray of the prior art is now formulated, although the dispersibility is worsened it can be improved by a formulation of the composite powder of the present invention. Also, to control the inner pressure and dissolve the formulated product, a solvent as represented by an alcohol also can be formulated in the composition. Examples of such solvents are alcohol, n-pentane, isopentane, n-hexane, cyclohexane, isohexane, n-heptane, isooctane, 2,2-dimethylbutane, petroleum ether, petroleum benzene, ligroin, 2-pentene, methyl ethyl ether, and diethyl ether. Typically, inner pressure is 0.1 to 2.5 kg/cm2 G (gauge) at a temperature of 20 C.
  • The amount of propellant formulated is preferably 5 to 99% by weight of the total amount of the aerosol composition, more preferably 15 to 95% by weight. A good jetting state cannot be obtained at a level of less than 5% by weight.
  • In the composition of the present invention, in addition to the above components, any of the optional components known in the art can be formulated.
  • Examples of such formulation components include water; oils and fats such as avocado oil, almond oil, olive oil, grapeseed oil, sesame oil, Sasanqua oil, safflower oil, soybean oil, Tsubaki (camellia) oil, corn oil, rapeseed oil, persic oil, castor oil, sunflower oil, cottonseed oil, peanut oil, cacao oil, palm oil, coconut oil, tallow, fish fat, hardened oil, turtle oil, lard, mink oil, and egg yolk oil; waxes such as whale wax, shellac, beeswax, lanolin, liquid lanolin, carnauba wax, and canderilla wax; hydrocarbons such as liquid paraffin, liquid polyisobutylene, squalane, pristane, petrolatum, paraffin, and ceresin; silicone oils such as dimethyl polysiloxane, methyl phenyl polysiloxane, methylhydrogen polysiloxane, octamethyl cyclo tetrasiloxane, and decamethyl cyclopentasiloxane; fatty acids such as succinic acid, tartaric acid, citric acid, undecyleic acid, lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid, oleic acid, linoleic acid, ricinoleic acid, and behenic acid; alcohols such as ethanol, isopropanol, lauryl alcohol, cetanol, 2-hexyldecaol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, and lanolin alcohol; polyhydric alcohols such as ethylene glycol, diethylene glycol monoethyl ether, triethylene glycol, polyethylene glycol, propylene glycol, 1,3-butylene glycol, glycerine, and batyl alcohol; sugars such as glucose, sucrose, lactose, xylitol, sorbitol, mannitol, and maltitol; esters such as diisopropyl adipate, hexyldecyl isostearate, cetyl isooctanoate, olecyl oleate, decyl oleate, lanolin acetate, butyl stearate, isopropyl myristate, diethyl phthalate, and hexyl laurate; metal soaps such as aluminum stearate, magnesium stearate, zinc stearate, aluminum myristate, calcium myristate, magnesium myristate, zinc myristate, aluminum palmitate, calcium palmitate, magnesium palmitate, zinc paimitate, zinc laurate, zinc undecylate, and calcium acetate; natural water soluble polymeric compounds such as gum arabic, sodium alginate, casein, carageehnan, karaya gum, agar, quinceseed, gelatin, dextrin, starch, tragacanth, and pectin; natural dyes such as chlorophil and β-carotin; sorbitan monooleate, sorbitan monoisostearate, sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, sorbitan sesquioleate, sorbitan trioleate, diglycerol sorbitan penta-2-ethylhexylate, and diglycerol sorbitan tetra-2-ethylhexylate; glycerol polyglycerol fatty acids such as mono cottonseed oil fatty acid glycerol, monoerucic acid glycerol, sesquioleic acid glycerol, monostearic acid glycerol, a,a -oleic acid pyroglutamic acid glycerol, monostearic acid glycerol malic acid; propylene glycol fatty acid esters such as propylene glycerol monostearate; lipophilic nonionic surfactants such as hydrogenated castor oil derivatives, glycerol alkylethers; polyoxyethylene (i.e., POE) fatty acid esters such as POE sorbitan monooleate, POE sorbitan monostearate, POE sorbitan monooleate, POE sorbitan pentaoleate, and POE sorbitan tetraoleate; POE sorbitol fatty acid esters such as POE sorbitol monolaurate, POE sorbitol monooleate, POE sorbitol pentaoleate, POE sorbitol monostearate; POE glycerol fatty acid esters such as POE glycerol monostearate, POE glycerol monoisostearate, and POE glycerol triisostearate; POE fatty acid esters such as POE monooleate, POE distearate, POE monodioleate and ethylene glycol distearate; POE alkylethers such as POE lauryl ether, POE oleyl ether, POE stearyl ether, POE behenyl ether, POE 2-octyldodecyl ether, POE chlestanol ether; POE alkyl phenyl ethers such as POE octyl phenyl ether, POE nonyl phenyl ether, and POE dinonyl phenyl ether; Pluronic type surfactants such as Pluronic; POE*POP alkyl ethers such as POEOPOP cetyl ether, POEOPOP 2-decyl tetradecyl ether, POE*POP monobutyl ether, POE*POP hydrogenated lanolin, and POE' POP glycerol ether; tetra POE'tera POP ethylenediamine condensates such as Tetronic; POE castor oil hydrogenated castor oil derivatives such as POE castor oil, POE hydrogenated castor oil, POE hydrogenated castor oil monoisostearate, POE hydrogenated castor oil - isostearate, POE hydrogenated castor oil monopyroglutamic acid monoisostearic acid diester, and POE hydrogenated castor oil maleic acid; POE beeswax*lanolin derivatives such as POE sorbitol beeswax; alkanol amides such as coconut oil fatty acid diethanolamide, lauric acid monoethanol amide; hydrophilic nonionic surfactants such as POE propylene glycol fatty acid esters, POE alkylamines, POE fatty acid amides, sucrose fatty acid esters, POE nonylphenyl formaldehyde condensates, alkylethoxydimethyl amine oxides, and trioleyl phosphoric acid; fatty acid soaps such as soap bases, sodium laurate and sodium palmitate; higher alkyl sulfuric acid ester salts such as sodium lauryl sulfate, potassium lauryl sulfate; alkyl ether sulfuric acid ester salts such as POE lauryl sulfate triethanolamine and sodium POE lauryl sulfate; N-acyl sarcosinic acids such as sodium lauroyl sarcosinate; higher fatty acid amide sulfonic acid salts such as sodium N-myristoyl-N-methyl taurine, sodium coconut oil fatty acid methyltauride, and sodium lauryl methyltauride; phosphoric acid ester salts such as sodium POE oleyl ether phosphate and sodium POE stearyl ether phosphate; sulfosuccinic acid salts such as sodium di-2-ethylhexyl sulfosuccinate, sodium monolauroyl monoethanolamide polyoxyethylene sulfosuccinate, and sodium lauryl polypropyleneglycol sulfosuccinate; alkylbenzene sulfonic acid esters of, for example, linear dodecylbenzene sulfonic acid such as sodium linear dodecylbenzene sulfonate and triethanolamine linear dodecylbenzene sulfonate; N-acylglutamic acid salts such as monosodium N-lauroyl glutamic acid, disodium N-stearoyl glutamic acid, and monosodium N-myristoyl-L-glutamate; higher fatty acid ester sulfuric acid ester salts such as sodium hydrogenated coconut oil fatty acid glycerol sulfate; sulfated oil such as Turkey red oil; anionic surfactants such as POE alkyl ether carboxylic acids, POE alkyl allyl ether carboxylic acid salts, a-olefin sulfonic acid salts, higher fatty acid ester sulfonic acid salts, secondary alcohol sulfuric ester salts, higher fatty acid alkylolamide sulfuric acid ester salts, sodium lauroyl monoethanolamide succinate, N-palmytoyl aspartic acid ditriethanolamine, and sodium casein; silicone surfactants such as polyether modified silicone, amino modified silicone, alkyl modified silicone, alcohol modified silicone, and carboxylic acid modified silicone; fluorine containing surfactants such as perfluoroalkyl carboxylic acid salts, perfluoroalkyl phosphoric acid esters, perfluoroalkyl carboxylic acid salts, perfluoroalkyl trimethyl ammonium salts, perfluoroalkyl betains, perfluoroalkylamine oxide, and perfluoroalkyl EO addition products; preservatives such as butyl p-oxybenzoate, propyl p-oxybenzoate, and methyl p-oxybenzoate; vitamins such as vitamin A, vitamin D, vitamin E, and vitamin K; hormones such as estradiol, ethynylestradiol, and cortisone; antisweat agents such as aluminum hydroxychloride, aluminum chloride, aluminum sulfate, basic aluminum bromide, aluminum phenolsulfonic acid, tannic acid, aluminum naphthalenesulfonic acid, and basic aluminum iodide; UV-absorbers such as urocanic acid and cynoxate; antiphlogistics such as allantoin, aloe powder, and guaizulene; sterilizers such as 3,4,4-trichlorocarbanilide (T.C.C.), triethylcitrate (T.E.C.), benzalkonium chloride, benzotonium chloride, alkyltrimethylammonium chloride, resorcin, phenol, sorbic acid, salicylic acid, and hexachlorophen; essential oils which are natural plant perfumes such as lavender, lemon, jasmin, mint, peppermint, rose, and camphor; animal perfumes such as musk, civet, and castoreum, and other synthetic perfumes; and a compressed gas such as carbon dioxide gas, nitrogen gas, and nitrous oxide gas.
  • The present invention provides an aerosol composition having an excellent powder dispersibility and useability by reducing the amount of Freon gas or without using Freon gas, and thus meets current requirements to restrict the use of this gas due to its influence on the ozone layer.
  • Examples
  • The present invention will now be further illustrated by, but is by no means limited to, the following Examples, wherein all parts and percentages are expressed on a weight basis unless otherwise noted.
  • Evaluation test methods used hereinbelow will be described.
  • Powder dispersibility test
  • Powder and a propellant were filled in an aerosol glass bottle, and after shaking, the time in which the powder sedimented at the bottom of the bottle was measured.
  • Useability test
  • Each sample was sprayed on the forearm for 3 seconds, and the extendability of the powder was evaluated. The evaluation standards are as follows.
    • o ... very well extended and free flowing
    • o ... slightly extended and free flowing
    • A ... not well extended
    • x ... very poorly extended
    Examples 1 - 2 and Comparative Examples 1 - 4
  • Table 1 shows Examples and Comparative Examples.
    Figure imgb0001
  • As shown in Table 1, in Examples 1 and 2, the time taken for the powder to precipitate after shaking was remarkably lengthened. In the case of the propellant liquid with a specific gravity of 1.2 or less, those formulated with the composite powder had an extremely good dispersibility, with the sedimentation time being prolonged 3-fold to 4-fold compared to the silica formulated product of the Comparative Examples. Also, the useability of the present Examples was found to be significantly better, compared with Comparative Examples formulated with conventional silica.
  • Example 3: Deodorant Spray
  • Figure imgb0002
  • After the components (1) to (5) were filled in an aerosol can, a valve was mounted and crimped, and the components (6) to (8) were filled under pressure to obtain a deodorant spray. The spray had a good powder dispersibility and useability.
  • Example 4: Cologne Powder Spray
  • Figure imgb0003
  • After (1) to (3) were filled in an aerosol can, a valve was mounted and crimped, and the components (4) and (5) were filled under pressure to obtain a cologne powder spray. The spray was found to have a good powder dispersibility.and useability.
  • Example 5: Deodorant Spray
  • Figure imgb0004
  • After the components (1) to (5) were filled in an aerosol can, a valve was mounted and crimped, and the components (6) and (7) were filled under pressure to obtain a deodorant spray. The spray was found to have a good powder dispersibility and useability.
  • Example 6: Powder Cologne Spray
  • Figure imgb0005
  • After the components (1) to (6) were homogeneously mixed, the mixture was filled in an aerosol can and a valve was mounted and crimped. After crimping, (7) was filled under pressure to obtain a powder cologne spray. The spray was found to have a good powder dispersibility and useability.
  • Example 7: Deodorant Powder Spray
  • Figure imgb0006
  • The components (1) to (6) were homogeneously mixed and then filled in a aerosol can, and a valve was mounted and crimped, followed by filling (7) and (8) to obtain a deodorant powder spray. The spray was found to have a good powder dispersibility and useability.
  • Example 8: Powder Spray
  • Figure imgb0007
  • After the components (1) to (5) were mixed, the mixture was filled in an aerosol can, and a valve was mounted and crimped, followed by filling (6) and (7) under pressure to obtain a powder spray. The spray was found to have a good powder dispersibility and useability.
  • Example 9: Powder Spray for Systemic Use
  • Figure imgb0008
  • A solution of (2) to (4) dissolved in the components (1) and (5) was filled in an aerosol can and a valve was mounted and crimped, followed by filling (6) and (7) under pressure to obtain a powder spray for systemic use. The spray was found to have a good powder dispersibility and useability.
  • Example 10: Deodorant Cologne Spray
  • Figure imgb0009
  • After (2), (6) and (7) were dissolved in the components (1) and (3), (4) and (5) were added, and the mixture filled in an aerosol can. A valve was mounted and crimped, followed by filling (8) and (9) under pressure to obtain a deodorant cologne spray. The spray was found to have a good powder dispersibility and useability.
  • Example 11: Deodorant Powder Spray
  • Figure imgb0010
  • After the components (1) to (4) were homogeneously mixed, the mixture was filled in an aerosol can. A valve was mounted and crimped, followed by filling (5) and (6) under pressure to obtain a deodorant powder spray. The spray was found to have a good powder dispersibility and useability.
  • Example 12: Deodorant Spray
  • Figure imgb0011
  • After the components (1) to (4) were uniformly mixed and filled in an aerosol can, a valve was mounted and crimped, and the component (5) was filled under pressure to obtain a deodorant spray.
  • Example 13: Cologne Powder Spray
  • Figure imgb0012
  • After (1) to (3) were filled in an aerosol can, a valve was mounted and crimped, and the components (4) and (5) were filled under pressure to obtain a cologne powder spray.
  • Example 14: Foot Spray
  • Figure imgb0013
  • After (1) to (4) were uniformly mixed and filled in an aerosol can, a valve was mounted and crimped, and the component (5) was filled under pressure to obtain a foot spray.
  • The powder dispersibility and useability of the products obtained in Examples 12, 13, and 14 were evaluated as mentioned above. The results are shown in Table 2.
    Figure imgb0014
  • As is clear from the results shown in Table 2, the products of Examples 12 to 14 had an excellent dispersibility and useability.
  • Example 15: Deodorant Spray
  • Figure imgb0015
  • After the components (1) to (5) were uniformly mixed and filled in an aerosol can, a valve was mounted and crimped, and the component (6) was filled under pressure to obtain a deodorant spray. The spray obtained was found to have a good powder dispersibility, useability, and deodorizing property.
  • Example 16: Powder Spray
  • Figure imgb0016
    Figure imgb0017
  • After the components (1) to (3) were uniformly mixed and filled in an aerosol can, a valve was mounted and crimped. After crimping, the component (4) was filled under pressure to obtain a powder spray. The spray was found to have a good powder dispersibility and useability.
  • Example 17: Powder Spray for Systemic Use
  • Figure imgb0018
  • After the components (1) to (5) were mixed, the mixture was filled in an aerosol can, and a valve was mounted and crimped, followed by filling (6) and (7) under pressure to obtain a powder spray. The spray was found to have a good powder dispersibility and useability.
  • Example 18: Powder Spray
  • Figure imgb0019
  • The components (1) and (2) and the components (3) and (4) were separately uniformly mixed. The resultant mixtures and the component (5) were then filled in an aerosol can, and a valve was mounted and crimped, followed by filling the component (6) under pressure to obtain a powder spray.
  • Example 19: Foot Spray
  • Figure imgb0020
  • The components (1) to (3) and the components (4) and (5) were separately uniformly mixed and then filled, together with the component (6), in an aerosol can, and a valve was mounted and crimped, followed by filling the component (7) under pressure to obtain a foot spray.

Claims (7)

1. An aerosol composition comprising a composite powder and at least one propellant selected from the group consisting of propane, n-butane, isobutane, a liquefied petroleum gas, a chlorinated hydrocarbon, and dimethyl ether.
2. An aerosol composition as claimed in claim 1, further comprising a Freon gas.
3. An aerosol composition as claimed in claim 1, wherein the composite powder comprises a core powder coated on the surface thereof with a sheath powder.
4. An aerosol composition comprising at least one propellant selected from the group consisting of propane, n-butane, isobutane, and a liquefied petroleum gas, at least one solvent selected from the group consisting of n-pentane, isopentane, and n-hexane, and a composite powder.
5. An aerosol composition as claimed in claim 4, wherein the vapor pressure of a mixture of the propellant and the solvent is 0.1 to 2.5 kg/cm2G at 20" C.
6. An aerosol composition as claimed in claim 4, further comprising a Freon gas.
7. An aerosol composition as claimed in claim 4, wherein the composite powder comprises a core powder coated on the surface thereof with a sheath powder.
EP89305990A 1988-06-20 1989-06-13 Aerosol composition Expired - Lifetime EP0348091B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP150194/88 1988-06-20
JP15019488 1988-06-20
JP255401/88 1988-10-11
JP25540188 1988-10-11

Publications (2)

Publication Number Publication Date
EP0348091A1 true EP0348091A1 (en) 1989-12-27
EP0348091B1 EP0348091B1 (en) 1994-01-12

Family

ID=26479879

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89305990A Expired - Lifetime EP0348091B1 (en) 1988-06-20 1989-06-13 Aerosol composition

Country Status (7)

Country Link
EP (1) EP0348091B1 (en)
JP (1) JP2896902B2 (en)
KR (1) KR930002223B1 (en)
AU (1) AU620877B2 (en)
CA (1) CA1338876C (en)
DE (1) DE68912215T2 (en)
ES (1) ES2061994T3 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2755858A1 (en) * 1996-11-20 1998-05-22 Harajon Isabelle Compositions for treating skin irritation in babies
WO2003057181A1 (en) * 2001-12-26 2003-07-17 The Gillette Company Packaging means for personal care products
WO2009151572A3 (en) * 2008-06-13 2010-07-29 S. C. Johnson & Son, Inc. Compositions containing a solvated active agent suitable for dispensing as a compressed gas aerosol
CN102317400A (en) * 2008-12-18 2012-01-11 3M创新有限公司 The method for preparing the hydridization gas gel

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3725567B2 (en) * 1994-01-19 2005-12-14 株式会社ダイゾー Atomized aerosol composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3494871A (en) * 1966-01-03 1970-02-10 Aerosol Tech Inc Chemiluminescent aerosols
GB2029441A (en) * 1978-08-21 1980-03-19 Toyo Aerosol Ind Co Powder aerosol composition

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU437703B2 (en) * 1970-03-10 1973-07-04 The Mennen Company Perspiration responsive aerosol deodorant
US4110427A (en) * 1976-04-14 1978-08-29 The Risdon Manufacturing Company Powdered solid aerosol composition and method of manufacture
GB1591312A (en) * 1976-10-28 1981-06-17 Unilever Ltd Aerosol package
US4328319A (en) * 1980-10-27 1982-05-04 Restech Research Limited Partnership Process for preparing propellant compositions forming foamed structures containing open and/or closed cells
JPS57174398A (en) * 1981-04-21 1982-10-27 Toyo Carbon Kk Aerosol-type graphite dispersion
JPS58103301A (en) * 1981-12-14 1983-06-20 Toyo Aerosol Kogyo Kk Powdery aerosol suspension liquid
JPS6047090A (en) * 1983-08-25 1985-03-14 Toyo Aerosol Kogyo Kk Powder aerosol composition
JPS60215092A (en) * 1984-04-09 1985-10-28 Kao Corp Powdery aerosol composition to be applied to the human body
JPS62148586A (en) * 1985-12-24 1987-07-02 Toyo Aerosol Kogyo Kk Powder aerosol composition
EP0251462A3 (en) * 1986-05-28 1988-10-26 Lloyd I. Osipow Polymer-propellant compositions forming foamed structures

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3494871A (en) * 1966-01-03 1970-02-10 Aerosol Tech Inc Chemiluminescent aerosols
GB2029441A (en) * 1978-08-21 1980-03-19 Toyo Aerosol Ind Co Powder aerosol composition

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
SEIFEN-OLE-FETRE-WACHSE, vol. 98, no. 15, 20th July 1972, pages 489-491; W. LANZENDORF: "Aerosole-technische Hinweise zu Puderaerosolen und Aerosol-Treibmitteln" *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2755858A1 (en) * 1996-11-20 1998-05-22 Harajon Isabelle Compositions for treating skin irritation in babies
WO2003057181A1 (en) * 2001-12-26 2003-07-17 The Gillette Company Packaging means for personal care products
WO2009151572A3 (en) * 2008-06-13 2010-07-29 S. C. Johnson & Son, Inc. Compositions containing a solvated active agent suitable for dispensing as a compressed gas aerosol
US8178078B2 (en) 2008-06-13 2012-05-15 S.C. Johnson & Son, Inc. Compositions containing a solvated active agent suitable for dispensing as a compressed gas aerosol
AU2009258191B2 (en) * 2008-06-13 2012-11-08 S.C. Johnson & Son, Inc. Compositions containing a solvated active agent suitable for dispensing as a compressed gas aerosol
US9044414B2 (en) 2008-06-13 2015-06-02 S.C. Johnson & Son, Inc. Compositions containing a solvated active agent for dispensing as a gas aerosol
CN102317400A (en) * 2008-12-18 2012-01-11 3M创新有限公司 The method for preparing the hydridization gas gel

Also Published As

Publication number Publication date
JPH02191693A (en) 1990-07-27
AU3667789A (en) 1989-12-21
CA1338876C (en) 1997-01-28
DE68912215D1 (en) 1994-02-24
ES2061994T3 (en) 1994-12-16
AU620877B2 (en) 1992-02-27
KR910000985A (en) 1991-01-30
EP0348091B1 (en) 1994-01-12
KR930002223B1 (en) 1993-03-27
DE68912215T2 (en) 1994-06-09
JP2896902B2 (en) 1999-05-31

Similar Documents

Publication Publication Date Title
US5223244A (en) Aerosol composition
US5665368A (en) Sprayable compositions containing dispersed powders and methods for using the same
US4605554A (en) Roll-on application of aqueous microencapsulated products
JPH04266808A (en) Cosmetic composition in form of hollow microsphere containing solid powder
US7303767B2 (en) Personal care compositions comprising coated/treated metal silicate absorbent particles
CA2066417C (en) Antiperspirant
US5800805A (en) Aerosol deodorant product
WO1996017583A1 (en) Solid cosmetic composition
JPH03204803A (en) Adsorbent for peroxylipid
US7303766B2 (en) Coated/treated metal silicate absorbent particles
JP2893541B2 (en) Hydrotalcite coated powder
EP0348091B1 (en) Aerosol composition
JP2938484B2 (en) Cosmetic for skin external or head
JPH06166611A (en) Powdery cosmetic
JPH01143820A (en) Deodorant
US5156833A (en) Powder aerosol composition
JP2000327527A (en) Solid water-in-oil type emulsion cosmetic
JPH01308819A (en) Magnesium metasilicatealuminate-coated powder and dermal ointment, deodorant and oral composition using same
JP2002241230A (en) Solid powder cosmetic
JPH05285370A (en) Water and oil repellent powder and cosmetic containing the same
JPH0648919A (en) Powder-containing aerosol composition
JP2896906B2 (en) Head composition
JPH0539209A (en) Complex cosmetic powder and cosmetic containing the same powder
JPH08245343A (en) Composite powder and cosmetic
JPH0395289A (en) Aerosol composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19890625

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE ES FR GB IT NL

17Q First examination report despatched

Effective date: 19920326

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE ES FR GB IT NL

ITF It: translation for a ep patent filed

Owner name: JACOBACCI CASETTA & PERANI S.P.A.

REF Corresponds to:

Ref document number: 68912215

Country of ref document: DE

Date of ref document: 19940224

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2061994

Country of ref document: ES

Kind code of ref document: T3

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20040507

Year of fee payment: 16

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20040603

Year of fee payment: 16

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20040628

Year of fee payment: 16

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050613

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050614

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20060101

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20050613

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20060101

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20050614

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20080621

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20080626

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20080514

Year of fee payment: 20